Dme-Hsa Disease Database (DHDD): Conserved Human Disease-Related miRNA and Their Targeting Genes in Drosophila melanogaster.
Dme-Hsa Disease Database (DHDD): Conserved Human Disease-Related miRNA and Their Targeting Genes in Drosophila melanogaster.
复制标题
Dme-Hsa 疾病数据库 (DHDD):果蝇中保守的人类疾病相关 miRNA 及其靶向基因
DOI:
10.3390/ijms19092642
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发表时间:
2018-09-06
影响因子:
5.6
通讯作者:
Ma F
中科院分区:
文献类型:
--
作者:
Wei G;Sun L;Qin S;Li R;Chen L;Jin P;Ma F
Abnormal expressions of microRNA (miRNA) can result in human diseases such as cancer and neurodegenerative diseases. MiRNA mainly exert their biological functions via repressing the expression of their target genes. Drosophila melanogaster (D. melanogaster) is an ideal model for studying the molecular mechanisms behind biological phenotypes, including human diseases. In this study, we collected human and D. melanogaster miRNA as well as known human disease-related genes. In total, we identified 136 human disease-related miRNA that are orthologous to 83 D. melanogaster miRNA by mapping “seed sequence”, and 677 human disease-related genes that are orthologous to 734 D. melanogaster genes using the DRSC Integrative Ortholog Prediction Tool Furthermore, we revealed the target relationship between genes and miRNA using miRTarBase database and target prediction software, including miRanda and TargetScan. In addition, we visualized interaction networks and signalling pathways for these filtered miRNA and target genes. Finally, we compiled all the above data and information to generate a database designated DHDD This is the first comprehensive collection of human disease-related miRNA and their targeting genes conserved in a D. melanogaster database. The DHDD provides a resource for easily searching human disease-related miRNA and their disease-related target genes as well as their orthologs in D. melanogaster, and conveniently identifying the regulatory relationships among them in the form of a visual network.
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DOI:
10.1146/annurev.pathol.3.121806.151529
发表时间:
2009
期刊:
Annual review of pathology
影响因子:
--
作者:
Lu B;Vogel H
通讯作者:
Vogel H
影响因子:
2.7
作者:
Gao, XS;Neufeld, TP;Pan, DJ
通讯作者:
Pan, DJ
影响因子:
14.9
作者:
Betel D;Wilson M;Gabow A;Marks DS;Sander C
通讯作者:
Sander C
影响因子:
14.9
作者:
Chien, S;Reiter, LT;Gribskov, M
通讯作者:
Gribskov, M
影响因子:
14.9
作者:
Jiang Q;Wang Y;Hao Y;Juan L;Teng M;Zhang X;Li M;Wang G;Liu Y
通讯作者:
Liu Y